The MACSima™ Instrument is a fully automated imaging system based on fluorescence microscopy. It’s MICS (multiparameter imaging cell screen) technology united with a broad spectrum of available antibodies, enables you to analyze hundreds of markers within a single sample, multiple samples at a time, while it is still convenient and easy to use. The technology uses the basic principle of iterative staining with different fluorochrome-conjugated antibodies to acquire microscopy data for a multitude of parameters without harming the sample. The resulting stack of hundreds of marker images provides an unprecedented insight into any kind of fixed sample.,In this interview Dr. Ali Ertürk, Director of the Institute for Tissue Engineering and Regenerative Medicine (iTERM), Helmholtz Zentrum Münche

The MACSima™ Instrument is a fully automated imaging system based on fluorescence microscopy. It’s MICS (multiparameter imaging cell screen) technology united with a broad spectrum of available antibodies, enables you to analyze hundreds of markers within a single sample, multiple samples at a time, while it is still convenient and easy to use. The technology uses the basic principle of iterative staining with different fluorochrome-conjugated antibodies to acquire microscopy data for a multitude of parameters without harming the sample. The resulting stack of hundreds of marker images provides an unprecedented insight into any kind of fixed sample.,In this interview Dr. Ali Ertürk, Director of the Institute for Tissue Engineering and Regenerative Medicine (iTERM), Helmholtz Zentrum Münche

Crawling of effector CD8 T (CD8 TE) cells visualized by multiphoton intravital microscopy in the liver of a HBcAg transgenic mouse (H2b) that was injected with H2b-restricted Cor93 (red) and H2d-restricted Env28 (green) CD8 TE. Sinusoids are in gray and hepatocellular nuclei are in blue. Scale bar represents 50 mm. Observations indicate that CD8 TE exhibit an intrasinusoidal crawling behavior that halts when hepatocellular antigens are recognized. The data was kindly provided by Matteo Iannacone, San Raffaele Scientific Institute, Milan.

Enter new territories using the UltraMicroscope Blaze™. With the fully automated light sheet microscope you will gain new insights as you can image an entire mouse or multiple organs and organoids with subcellular resolution in 3D. The combination of our pioneering UltraMicroscope technology with cutting-edge optics ensures excellent data quality allowing you to dive deep into the details. The UltraMicroscope Blaze is the fully automated light sheet microscope for imaging very large or multiple samples utilizing advanced optics ensuring excellent data quality